Works matching IS 09646906 AND DT 2002 AND VI 11 AND IP 17

Results: 15

Altered transcriptional regulation in cells expressing the expanded polyglutamine androgen receptor.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1967, doi. 10.1093/hmg/11.17.1967

By:

Lieberman, Andrew P.;
Harmison, George;
Strand, Andrew D.;
Olson, James M.;
Fischbeck, Kenneth H.

Publication type:

Article

A regression-based method to identify differentially expressed genes in microarray time course studies and its application in an inducible Huntington's disease transgenic model.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1977

By:

Xu, Xie L.;
Olson, James M.;
Zhao, Lue Ping

Publication type:

Article

Early transcriptional profiles in huntingtin-inducible striatal cells by microarray analyses.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1953, doi. 10.1093/hmg/11.17.1953

By:

Sipione, Simonetta;
Rigamonti, Dorotea;
Valenza, Marta;
Zuccato, Chiara;
Conti, Luciano;
Pritchard, Joel;
Kooperberg, Charles;
Olson, James M.;
Cattaneo, Elena

Publication type:

Article

Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 2005

By:

Di, Wei-Li;
Monypenny, James;
Common, John E.A.;
Kennedy, Cameron T.C.;
Holland, Katalin A.;
Leigh, Irene M.;
Rugg, Elizabeth L.;
Zicha, Daniel;
Kelsell, David P.

Publication type:

Article

Microarrays and polyglutamine disorders: reports from the Hereditary Disease Array Group.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1909, doi. 10.1093/hmg/11.17.1909

By:

Orr, Harry T.

Publication type:

Article

Polyglutamine and transcription: gene expression changes shared by DRPLA and Huntington's disease mouse models reveal context-independent effects.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1927, doi. 10.1093/hmg/11.17.1927

By:

Luthi-Carter, Ruth;
Strand, Andrew D.;
Hanson, Sarah A.;
Kooperberg, Charles;
Schilling, Gabriele;
La Spada, Albert R.;
Merry, Diane E.;
Young, Anne B.;
Ross, Christopher A.;
Borchelt, David R.;
Olson, James M.

Publication type:

Article

Dysregulation of gene expression in the R6/2 model of polyglutamine disease: parallel changes in muscle and brain.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1911, doi. 10.1093/hmg/11.17.1911

By:

Luthi-Carter, Ruth;
Hanson, Sarah A.;
Strand, Andrew D.;
Bergstrom, Donald A.;
Chun, Wanjoo;
Peters, Nikki L.;
Woods, Annette M.;
Chan, Edmond Y.;
Kooperberg, Charles;
Krainc, Dimitri;
Young, Anne B.;
Tapscott, Stephen J.;
Olson, James M.

Publication type:

Article

hnRNP-G promotes exon 7 inclusion of survival motor neuron (SMN) via direct interaction with Htra2-β1.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 2037, doi. 10.1093/hmg/11.17.2037

By:

Hofmann, Yvonne;
Wirth, Brunhilde

Publication type:

Article

Specific haplotypes of the P-selectin gene are associated with myocardial infarction.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 2015, doi. 10.1093/hmg/11.17.2015

By:

Tregouet, David-Alexandre;
Barbaux, Sandrine;
Escolano, Sylvie;
Tahri, Nadia;
Golmard, Jean-Louis;
Tiret, Laurence;
Cambien, François

Publication type:

Article

Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's disease.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1939, doi. 10.1093/hmg/11.17.1939

By:

Chan, Edmond Y.W.;
Luthi-Carter, Ruth;
Strand, Andrew;
Solano, Steven M.;
Hanson, Sarah A.;
DeJohn, Molly M.;
Kooperberg, Charles;
Chase, Kathryn O.;
DiFiglia, Marian;
Young, Anne B.;
Leavitt, Blair R.;
Cha, Jang-Ho J.;
Aronin, Neil;
Hayden, Michael R.;
Olson, James M.

Publication type:

Article

The yeast frataxin homolog Yfh1p plays a specific role in the maturation of cellular Fe/S proteins.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 2025, doi. 10.1093/hmg/11.17.2025

By:

Mühlenhoff, Ulrich;
Richhardt, Nadine;
Ristow, Michael;
Kispal, Gyula;
Lill, Roland

Publication type:

Article

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1987, doi. 10.1093/hmg/11.17.1987

By:

Estivill, Xavier;
Cheung, Joseph;
Angel Pujana, Miguel;
Nakabayashi, Kazuhiko;
Scherer, Stephen W.;
Tsui, Lap-Chee

Publication type:

Article

A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 2051, doi. 10.1093/hmg/11.17.2051

By:

Castanet, Mireille;
Park, Soo-Mi;
Smith, Aaron;
Bost, Michel;
Léger, Juliane;
Lyonnet, Stanislas;
Pelet, Anna;
Czernichow, Paul;
Chatterjee, Krishna;
Polak, Michel

Publication type:

Article

Differential gene expression in a cell culture model of SOD1-related familial motor neurone disease.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 2061, doi. 10.1093/hmg/11.17.2061

By:

Kirby (née Tomkins), Janine;
Menzies, Fiona M.;
Cookson, Mark R.;
Bushby, Katherine;
Shaw, Pamela J.

Publication type:

Article

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1997, doi. 10.1093/hmg/11.17.1997

By:

Challis, Benjamin G.;
Pritchard, Lynn E.;
Creemers, John W.M.;
Delplanque, Jerome;
Keogh, Julia M.;
Luan, Jian'an;
Wareham, Nicholas J.;
Yeo, Giles S.H.;
Bhattacharyya, Sumit;
Froguel, Phillipe;
White, Anne;
Farooqi, I. Sadaf;
O'Rahilly, Stephen

Publication type:

Article